Cas 956093-30-4,5'-O-(4,4'-dimethoxytrityl)-3'-O-[(6-bromohexyl)-N,N-diisopropylaminophosphoramidite]thymidine

956093-30-4

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Basic information

Product Name: 5'-O-(4,4'-dimethoxytrityl)-3'-O-[(6-bromohexyl)-N,N-diisopropylaminophosphoramidite]thymidine
Synonyms: 5'-O-(4,4'-dimethoxytrityl)-3'-O-[(6-bromohexyl)-N,N-diisopropylaminophosphoramidite]thymidine
CAS NO:956093-30-4
Molecular Formula:
Molecular Weight: 854.819
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5'-O-(4,4'-dimethoxytrityl)-3'-O-[(6-bromohexyl)-N,N-diisopropylaminophosphoramidite]thymidine(CAS DataBase Reference)
NIST Chemistry Reference: 5'-O-(4,4'-dimethoxytrityl)-3'-O-[(6-bromohexyl)-N,N-diisopropylaminophosphoramidite]thymidine(956093-30-4)
EPA Substance Registry System: 5'-O-(4,4'-dimethoxytrityl)-3'-O-[(6-bromohexyl)-N,N-diisopropylaminophosphoramidite]thymidine(956093-30-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 956093-30-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 956093-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,0,9 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 956093-30:
(8*9)+(7*5)+(6*6)+(5*0)+(4*9)+(3*3)+(2*3)+(1*0)=194
194 % 10 = 4
So 956093-30-4 is a valid CAS Registry Number.

956093-30-4Upstream product

956093-30-4Downstream Products

956093-30-4Relevant academic research and scientific papers

New strategies for cyclization and bicyclization of oligonucleotides by click chemistry assisted by microwaves

Lietard, Jory,Meyer, Albert,Vasseur, Jean-Jacques,Morvan, Francois

, p. 191 - 200 (2008)

(Chemical Equation Presented) The synthesis of cyclic, branched, and bicyclic oligonucleotides was performed by copper-catalyzed azide-alkyne cycloaddition assisted by microwaves in solution and on solid support. For that purpose, new phosphoramidite buil

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